Canonical Allele Identifier: PA2828414317
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 579558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ser1367Asn
CA394300256
NM_001370404.1:c.4100G>A